CHISEL (OSTEOTOME, GOUGE, ETC.)

CHISEL (OSTEOTOME, GOUGE, ETC.) is an FDA 510(k)-cleared medical device (K864775) manufactured by New England Surgical Instrument Corp.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 11, 1987. Regulation: 8.